Jobs / United States / Glaxosmithkline LLC
Pharmacovigilance Associate
Glaxosmithkline LLC · 🇺🇸 Petach Tikvah
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 39 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 15 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Glaxosmithkline LLC paid sponsored hires in similar roles4 certified filings for “Associate Director – Genomic Technologies” (Molecular and Cellular Biologists) in PA: $134k–$138k, median $136k. Most were filed at wage level IV (50%) — 4 lottery entries, ≈61% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Glaxosmithkline LLC
The US Department of Labor certified 39 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 15 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Glaxosmithkline LLC →
About the role
GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems. Our diverse portfolio consists of vaccines, specialty medicines, and general medicines. Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges. Position Summary You will support the pharmacovigilance (PV) team in Israel by ensuring safety data and related systems are accurate and compliant. You will work closely with global and local colleagues, vendors and partners to process safety information, maintain PV records, and support reporting activities. We value accuracy, clear communication and a collaborative mindset. This role offers growth, meaningful impact on patient safety, and alignment with GSK’s mission of uniting science, technology and talent to get ahead of disease together. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Review, extract and accurately monitor adverse event (AE) data from spontaneous and solicited sources in the safety databases according to procedures. - Perform quality checks, reconciliations and basic case triage to ensure data completeness and timeliness. - Maintain and update pharmacovigilance agreements, safety documentation and document repositories. - Run database listings and reports; support metric collection and basic trend checks. - Liaise with local operating companies, vendors and internal teams to gather information and resolve data queries. - Provide administrative and system support for PV processes, including mailbox triage and document archiving. Why You? Basic Qualifications & Skills We are seeking professionals with the following required skills and qualifications to help us achieve our goals: - Pharmacist with Israeli license. - 1–4 years’ experience in pharmacovigilance / drug safety. - Strong attention to detail and experience with data entry, reconciliation or database work. - Good IT skills, including Excel and experience with web-based applications or safety databases. - Ability to communicate clearly in Hebrew and English, both written and verbal. - Comfortable working in a matrixed team and responding to stakeholders in a timely way. Preferred Qualifications & Skills If you have the following characteristics, it would be a plus: - Experience with ICSR (Individual Case Safety Report) processing. - Knowledge of local regulatory reporting requirements and pharmacovigilance methodology. - Prior experience with safety databases (e.g., Argus, Veeva or similar) or document management systems. - Experience working with vendors or in quality and compliance activities. - Demonstrated experience in process improvement or KPI analysis. Working arrangements This role is hybrid. You will be expected to work on-site in Israel regularly and have flexibility for remote working as agreed with your manager. How to apply If this role matches your skills and ambitions, we encourage you to apply. Tell us how your experience fits the responsibilities and qualifications. We look forward to hearing how you can contribute to patient safety and grow with our team. Skills Digital Fluency, Drug Safety Surveillance, Pharmacovigilance Why GSK? Uniting science, technology and talent to get ahead of diseas